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rs1057519885

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519885(C;T)
Make rs1057519885(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position20052443
GeneCFAP61, CRNKL1
is asnp
is mentioned by
dbSNPrs1057519885
dbSNP (old)rs1057519885
ClinGenrs1057519885
ebirs1057519885
HLIrs1057519885
Exacrs1057519885
Gnomadrs1057519885
Varsomers1057519885
Maprs1057519885
PheGenIrs1057519885
Biobankrs1057519885
1000 genomesrs1057519885
hgdprs1057519885
ensemblrs1057519885
gopubmedrs1057519885
geneviewrs1057519885
scholarrs1057519885
googlers1057519885
pharmgkbrs1057519885
gwascentralrs1057519885
openSNPrs1057519885
23andMers1057519885
23andMe allrs1057519885
SNPshotrs1057519885
SNPdbers1057519885
MSV3drs1057519885
GWAS Ctlgrs1057519885
Max Magnitude0
ClinVar
Risk rs1057519885(T;T)
Alt rs1057519885(T;T)
Reference Rs1057519885(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Squamous cell carcinoma of the skin
Variation info
Gene CFAP61 CRNKL1 C20orf26
CLNDBN Malignant melanoma of skin Squamous cell carcinoma of the skin
Reversed 1
HGVS NC_000020.10:g.20033087G>A
CLNSRC
CLNACC RCV000421158.1, RCV000431829.1,